Structure of the O‐specific polysaccharide of Proteus mirabilis D52 and typing of this strain to Proteus serogroup O33
Author(s) -
Zych Krystyna,
Toukach Filip V.,
Arbatsky Nikolay P.,
Kołodziejska Katarzyna,
Senchenkova Sof'ya N.,
Shashkov Alexander S.,
Knirel Yuriy A.,
Sidorczyk Zygmunt
Publication year - 2001
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1046/j.1432-1327.2001.02356.x
Subject(s) - proteus mirabilis , strain (injury) , antiserum , chemistry , polysaccharide , octahedron , proteus , microbiology and biotechnology , stereochemistry , biology , crystallography , antigen , escherichia coli , biochemistry , anatomy , crystal structure , genetics , gene
The acidic O‐specific polysaccharide chain (O‐antigen) of the lipopolysaccharide (LPS) of Proteus mirabilis strain D52 was studied using chemical analyses along with 1 H‐NMR and 13 C‐NMR spectroscopy, including 2D COSY, TOCSY, ROESY, H‐detected 1 H, 13 C and 1 H, 31 P HMQC experiments. The polysaccharide was found to contain d ‐ribitol 5‐phosphate ( d ‐Rib‐ol‐5‐ P ) and ethanolamine phosphate (Etn‐ P ) and has the following structure This structure is identical with that of the O‐polysaccharide of P. mirabilis O33 strain 59/57, and, hence, P. mirabilis D52 belongs to the same Proteus serogroup O33. Serological studies with O‐antiserum against P. mirabilis D52 confirmed this but showed that the LPS species of P. mirabilis 59/57 and D52 are not identical, having different epitopes in the core region. A serological cross‐reactivity of P. mirabilis D52 O‐antiserum was observed with LPS of two other Proteus strains, P. mirabilis O16 and P. penneri 103, which have structurally different O‐polysaccharides. The role of charged groups, Rib‐ol‐5‐ P and Etn‐ P in the immunospecificity is discussed.
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